A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418975



Internal ID21076528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9890872..9892491hg38UCSC Ensembl
chr8:9748382..9750001hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381620
hg191620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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